Calcination Temperature Dependent Catalytic Activity and Stability of IrO2–Ta2O5Anodes for Oxygen Evolution Reaction in Aqueous Sulfate Electrolytes
Source abstract
Abstract
In this work, commercial IrO 2 -Ta 2 O 5 anodes with a certain composition calcined at three different temperatures were investigated. The results show that the calcination temperature has a significant influence on the electrocatalytic activity for the oxygen evolution reaction (OER). This is attributed to the influence of the calcination temperature on the surface microstructure including the crystallinity and the preferred orientation of IrO 2 crystallites of the IrO 2 -Ta 2 O 5 binary oxide formed. The surface morphology of the anodes was revealed as mud-cracks surrounded by flat areas containing several scattered IrO 2 nanocrystallites. The size of these nanocrystallites, which in turn contribute to the electrochemical active surface area, is dependent on calcination temperature. The (101)-surfaces of the IrO 2 were found to have higher catalytic activity than (110) IrO 2 with respect to the OER. The (101) IrO 2 planes were dominating at low or moderate calcination temperatures, whereas the (110) IrO 2 orientation was preferred at the highest calcination temperature. Accelerated lifetime tests of the investigated samples indicate that the (101) IrO 2 is more stable (110) IrO 2 during electrolysis. A moderate temperature is suggested as the best calcination temperature for this type of anode regarding the electrochemical active surface area, electrocatalytic activity and stability for OER in acidic aqueous electrolytes at operating conditions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (32)
Show source-provided references
1. 10.1007/BF0061435710.1007/BF00614357 ↗
2. 10.1016/0304-386X(75)90003-110.1016/0304-386X(75)90003-1 ↗
3. 10.1016/S0013-4686(00)00338-810.1016/S0013-4686(00)00338-8 ↗
4. 10.1016/0013-4686(84)85004-510.1016/0013-4686(84)85004-5 ↗
5. 10.1016/0013-4686(86)80153-010.1016/0013-4686(86)80153-0 ↗
6. 10.1016/0013-4686(94)85134-410.1016/0013-4686(94)85134-4 ↗
7. 10.1016/S0010-938X(01)00165-210.1016/S0010-938X(01)00165-2 ↗
8. 10.1016/S0010-938X(03)00108-210.1016/S0010-938X(03)00108-2 ↗
9. 10.1038/srep1216710.1038/srep12167 ↗
10. 10.1007/BF0102021910.1007/BF01020219 ↗
11. 10.1007/BF0024219410.1007/BF00242194 ↗
12. 10.1149/1.156947910.1149/1.1569479 ↗
13. 10.1016/0013-4686(91)85306-R10.1016/0013-4686(91)85306-R ↗
14. 10.1016/S0013-4686(98)00274-610.1016/S0013-4686(98)00274-6 ↗
15. 10.1149/1.310464610.1149/1.3104646 ↗
16. 10.1016/0013-4686(94)85134-410.1016/0013-4686(94)85134-4 ↗
17. 10.1016/S0010-938X(01)00165-210.1016/S0010-938X(01)00165-2 ↗
18. 10.1016/S0010-938X(03)00108-210.1016/S0010-938X(03)00108-2 ↗
19. 10.1038/srep1216710.1038/srep12167 ↗
20. 10.1149/2.0211609jes10.1149/2.0211609jes ↗
21. 10.1016/0013-4686(91)85306-R10.1016/0013-4686(91)85306-R ↗
22. 10.1016/j.ssi.2005.03.01210.1016/j.ssi.2005.03.012 ↗
23. 10.1063/1.293802810.1063/1.2938028 ↗
24. 10.1016/j.electacta.2008.10.00410.1016/j.electacta.2008.10.004 ↗
25. 10.1016/0013-4686(95)00002-V10.1016/0013-4686(95)00002-V ↗
26. Cullity B. D. , Elements of X-ray diffraction, Addison-Wesley (1956).
27. 10.1016/0079-6425(78)90003-810.1016/0079-6425(78)90003-8 ↗
28. Gale W. F. Owner T. C. , Smithells Metals Reference Book, p. 422.
29. 10.1023/A:101097522340510.1023/A:1010975223405 ↗
30. 10.1590/S0103-5053200300040002310.1590/S0103-50532003000400023 ↗
31. 10.1016/j.apsusc.2008.02.05410.1016/j.apsusc.2008.02.054 ↗
32. 10.1016/j.electacta.2015.01.00510.1016/j.electacta.2015.01.005 ↗